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Brain-age prediction: Systematic evaluation of site effects, and sample age range and size

  • ENIGMA-Lifespan Working Group
  • University of British Columbia
  • Icahn School of Medicine at Mount Sinai
  • University of British Columbia
  • Beijing Institute of Technology
  • Tsinghua University
  • Southwest University
  • Institute of Cell Biology and Neurobiology and IRCCS Santa Lucia Foundation
  • Vrije Universiteit Amsterdam
  • Indiana University School of Medicine
  • University of New South Wales
  • Harvard University
  • Harvard Medical School
  • Donders Institute for Brain, Cognition and Behaviour
  • MRC Centre for Neuropsychiatric Genetics and Genomics
  • University of New Mexico
  • Université de Montréal
  • Institut des Maladies Neurodégénératives
  • Leiden University
  • Erasmus School of Social and Behavioural Sciences
  • University of Münster
  • University of Melbourne
  • Amsterdam UMC
  • Queensland University of Technology
  • ASST Papa Giovanni Hospital Bergamo
  • Max Planck Institute for Psycholinguistics
  • Radboud University Nijmegen Medical Center
  • Heidelberg University
  • University of Pennsylvania
  • Sydney University Biological Informatics and Technology Centre (SUBIT)
  • Utrecht University
  • University Medical Centre Utrecht
  • Center for Human Development
  • Ohio State University College of Medicine
  • Institute of Mental Health
  • University of Barcelona
  • University of Texas
  • Montreal Neurological Institute
  • Charité – Universitätsmedizin Berlin
  • Fudan University
  • University of Bari Aldo Moro
  • Massachusetts General Hospital
  • University of Oslo
  • University of New South Wales
  • Medical College of Wisconsin
  • University of Bonn
  • King's College London
  • Keck School of Medicine of USC

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

34 Citations (Scopus)

Abstract

Structural neuroimaging data have been used to compute an estimate of the biological age of the brain (brain-age) which has been associated with other biologically and behaviorally meaningful measures of brain development and aging. The ongoing research interest in brain-age has highlighted the need for robust and publicly available brain-age models pre-trained on data from large samples of healthy individuals. To address this need we have previously released a developmental brain-age model. Here we expand this work to develop, empirically validate, and disseminate a pre-trained brain-age model to cover most of the human lifespan. To achieve this, we selected the best-performing model after systematically examining the impact of seven site harmonization strategies, age range, and sample size on brain-age prediction in a discovery sample of brain morphometric measures from 35,683 healthy individuals (age range: 5–90 years; 53.59% female). The pre-trained models were tested for cross-dataset generalizability in an independent sample comprising 2101 healthy individuals (age range: 8–80 years; 55.35% female) and for longitudinal consistency in a further sample comprising 377 healthy individuals (age range: 9–25 years; 49.87% female). This empirical examination yielded the following findings: (1) the accuracy of age prediction from morphometry data was higher when no site harmonization was applied; (2) dividing the discovery sample into two age-bins (5–40 and 40–90 years) provided a better balance between model accuracy and explained age variance than other alternatives; (3) model accuracy for brain-age prediction plateaued at a sample size exceeding 1600 participants. These findings have been incorporated into CentileBrain (https://centilebrain.org/#/brainAGE2), an open-science, web-based platform for individualized neuroimaging metrics.

Original languageEnglish
Article numbere26768
JournalHuman Brain Mapping
Volume45
Issue number10
DOIs
Publication statusPublished - 15 Jul 2024

Keywords

  • benchmarking
  • brain aging
  • brainAGE

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